rs12914385 associated_with Chrna3
Evidence from:
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all sources
Evidence (1 sources)
Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.
(2009)
PMID:19654303
cited
All three SNPs localise to intron 4 of CHRNA3 strongly favouring variation within this gene as being the basis of 15q25 lung cancer association.
confidence: 0.80